A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391746



Internal ID21049299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112614688..112664959hg38UCSC Ensembl
chr4:113535844..113586115hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3850272
hg1950272
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209554
Samples
Known GenesC4orf21, LARP7, MIR302A, MIR302B, MIR302C, MIR302D, MIR367
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391746
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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